The following data is part of a premarket notification filed by Bloomex International, Inc. with the FDA for Bx-400 Jesse Jimbody.
| Device ID | K813410 |
| 510k Number | K813410 |
| Device Name: | BX-400 JESSE JIMBODY |
| Classification | Stimulator, Muscle, Powered |
| Applicant | BLOOMEX INTERNATIONAL, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | IPF |
| CFR Regulation Number | 890.5850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-12-04 |
| Decision Date | 1982-03-08 |